22600-85-7

Usage

Uses

Used in Solvent Applications:
(5,5-diMethyltetrahydrofuran-3-yl)Methanol is used as a solvent in various industrial processes for its low toxicity and high boiling point, making it a safer and more efficient alternative to traditional solvents like diethyl ether and tetrahydrofuran.
Used in Organic Synthesis:
In the field of organic chemistry, (5,5-diMethyltetrahydrofuran-3-yl)Methanol serves as a reagent in numerous chemical reactions, taking advantage of its hydroxyl group and compatibility with a wide range of organic compounds.
Used in Chemical Reactions:
The presence of a hydroxyl group in its structure allows (5,5-diMethyltetrahydrofuran-3-yl)Methanol to be utilized in various chemical reactions, contributing to its popularity in industrial applications.
Safety Precautions:

Upstream product

• 53308-41-1 2-(2-methylallyl)propane-1,3-diol 
• 50598-40-8 dimethyl (2-methyl-2-propenyl)-propanedioate 
• 1575-67-3 2-(2-methyl-allyl)-malonic acid diethyl ester 

Downstream Products

• 926-56-7 4-methyl-1,3-pentadiene 
• 592-45-0 1,4-hexadiene 
• 926-54-5 trans-2-methyl-1,3-pentadiene 
• 4045-53-8 1,3-dimethylcyclopentadiene 
• 763-30-4 2-methyl-1,4-pentadiene 
• 5602-47-1 dimethyl-2,5 cyclopentadiene 

Relevant academic research and scientific papers

A convenient synthesis of 2-alkyl-2-methyltetrahydrofurans from 4- methylalk-4-en-1-ols catalyzed by iodine

Cyclization of 4-methylalk-4-en-1-ols in the presence of a catalytic amount of iodine in dichloromethane gave exclusively 2-alkyl-2- methyltetrahydrofurans under mild conditions in high yields.

6-HETEROARYLOXY BENZIMIDAZOLES AND AZABENZIMIDAZOLES AS JAK2 INHIBITORS

The present disclosure provides 6-heteroaryloxy benzimidazole and azabenzimidazole compounds and compositions thereof useful for inhibiting JAK2.

Catalytic Synthesis of Saturated Oxygen Heterocycles by Hydrofunctionalization of Unactivated Olefins: Unprotected and Protected Strategies

A mild, general, and functional group tolerant intramolecular hydroalkoxylation and hydroacyloxylation of unactivated olefins using a Co(salen) complex, an N-fluoropyridinium salt, and a disiloxane reagent is described. This reaction was carried out at ro

AROMATIC RING COMPOUND

Provided is an aromatic ring compound having a GPR40 agonist activity. A compound represented by the formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof has a GPR40 agonist activity, and is useful as an agent for the prophylaxis or treatment of diabetes and the like.

Intramolecular additions of alcohols and carboxylic acids to inert olefins catalyzed by silver(I) triflate

(Chemical Equation Presented) Intramolecular additions of hydroxyl or carboxyl groups to inert olefins catalyzed by simple silver(I) triflate are described. Good to excellent yields can be obtained for a range of substrates under relatively mild conditions. This reaction represents one of the simplest methods to construct cyclic ethers or lactones.